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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473887Generated: October 30, 2026

Potassium Carbonate → 2-(Imidazo[1,2-a]pyridin-8-ylmethoxy)-5-methoxybenzaldehyde

https://huagongshe.com/reaction/1473887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Hydroxy-5-methoxybenzaldehydeHCID 95695—
Reactant8-(Chloromethyl)imidazo[1,2-a]pyridineHCID 21661582—
SolventDimethylformamideHCID 6228—
Product2-(Imidazo[1,2-a]pyridin-8-ylmethoxy)-5-methoxybenzaldehydeHCID 7162146045%

Reaction Conditions

Temperature87.5 °C

Reaction Steps

To a solution of the crude 8-(chloromethyl)imidazo[1,2-a]pyridine (6.8 mmol, 1 eq) and 2-hydroxy-5-methoxybenzaldehyde (1.3 g, 8.1 mmol, 1.2 eq) in DMF (20 mL) was added potassium carbonate (2.8 g, 20.4 mmol, 3 eq) and the reaction mixture was heated at 85-90° C. for 5 h. DMF was removed under vacuum and the residue was taken in ethyl acetate and filtered. The solid was washed with additional ethyl acetate, and then dried and evaporated to give the crude, which was purified by column chromatography (EtOAc/Hexane) to yield the desired compound in 45% yield. NMR (400 MHz, CDCl3): δ 3.80 (s, 3H), 5.60 (s, 2H), 6.85 (d, 1H), 7.12 (d, 2H), 7.36 (m, 2H), 7.66 (m, 2H), 8.14 (m, 1H), 10.58 (s, 1H); MS: exact mass calculated for C16H14N2O3, 282.10; m/z found, 283 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018210B2
Source datasetuspto-grants-2015_04
ORD IDord-0eb5b9b6080743bdb70dd0e756544964
Source noteuspto-grants-2015_04